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Thermodynamics of polymer-diluent systems at high pressure.

机译:聚合物稀释剂系统在高压下的热力学。

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Diblock copolymers have enormous potential use as templating materials for the fabrication of highly ordered materials on a nanometer scale. This derives from the complexity of phase behavior in microphase-separated block copolymer systems. In the ordered state block copolymers commonly self-organize into ordered lamellae, cylinders or spheres. Recently, high-pressure diluents have been used as a processing aid when using block copolymers as a templating material. In this study several aspects of polymer-diluent phase behavior have been investigated using high-pressure carbon dioxide as a diluent.; It is well established that dilation of a copolymer changes the characteristic interdomain spacing of a phase-separated system. The interdomain spacing decreases with dilation by non-selective diluents and increases with selective diluents. The characteristic spacing of poly(styrene-block-dimethyl siloxane) has been measured using small angle neutron scattering (SANS) in high-pressure CO2. A new power-law scaling for the change in interdomain spacing induced by dilation, which accounts for selectivity of the diluent, is presented.; The effect of high-pressure carbon dioxide on the order-to-disorder transition (ODT) of poly(styrene-block-2-vinyl pyridine) has been investigated using static birefringence. The results of these experiments indicate that in addition to the suppression of the ODT, dilation of a copolymer by carbon dioxide can induce the appearance of a second morphology. Further the appearance of this second morphology is strongly dependant on the sample history.; Methods for measuring the swelling of homopolymers in carbon dioxide have also been investigated. High-pressure spectroscopic ellipsometry and laser interferometry have been developed as methods to measure the swelling of homopolymer films. It is shown that spectroscopic ellipsometry and laser interferometry are both capable of measuring the swelling of homopolymer films at high pressure.
机译:双嵌段共聚物作为模板材料具有巨大的潜在用途,可用于制备纳米级的高度有序的材料。这源于在微相分离的嵌段共聚物体系中相行为的复杂性。在有序状态下,嵌段共聚物通常自组织成有序的薄片,圆柱体或球体。近来,当使用嵌段共聚物作为模板材料时,高压稀释剂已被用作加工助剂。在这项研究中,使用高压二氧化碳作为稀释剂,研究了聚合物-稀释剂相行为的几个方面。公认的是,共聚物的膨胀改变了相分离体系的特征性畴间间距。域间间距随着非选择性稀释剂的膨胀而减小,而随着选择性稀释剂的增大而增大。聚(苯乙烯嵌段-二甲基硅氧烷)的特征间距已在高压CO2中使用小角度中子散射(SANS)进行了测量。提出了一种新的幂律定标,用于解释由膨胀引起的域间间距的变化,该变化解释了稀释剂的选择性。使用静态双折射研究了高压二氧化碳对聚(苯乙烯-嵌段-2-乙烯基吡啶)的有序到无序转变(ODT)的影响。这些实验的结果表明,除了抑制ODT外,二氧化碳对共聚物的膨胀还可以引起第二形态的出现。此外,第二种形态的出现在很大程度上取决于样品的历史。还研究了测量均聚物在二氧化碳中溶胀的方法。已经开发了高压光谱椭圆偏振法和激光干涉法作为测量均聚物膜溶胀的方法。结果表明,椭圆偏振光谱法和激光干涉法均能够测量高压下均聚物薄膜的溶胀。

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